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6 Oct 2022 / 3:00 pm - 3:45 pm

The New UK Regime for Goods: MHRA/BEIS: Medical Devices



Join BEIS and the Medicines and Healthcare products Regulatory Agency covering the requirements for the UKCA marking for medical devices.

Great Britain now has its own robust regulatory framework for goods, and manufacturers need to start using the UKCA marking. The UKCA regime seeks to ensure consumers are protected from unsafe, and non-compliant goods. Businesses should get ready for the new regime as soon as possible to ensure they are compliant by 1 January 2023.

For manufacturers placing medical devices on the UK market there is an extended transition period to 30th June 2023. Manufacturers should act now to understand the requirements and routes to conformity for The Medical Devices Regulations 2002 (SI 2002 N 618, as amended) (UK MDR).

In this session we will provide general guidance to medical device manufacturers on UKCA marking with focus on medical device specific requirements to provide clarity on the next steps required to maintain UK market access after June 2023.

There will also be a chance to ask questions at the end. Please note, we are unable to provide advice on your specific circumstances.

Register here